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Government Affairs Director

Role overview

Qualifications

  • Long-standing experience in life sciences government affairs, public policy, or related field
  • Experience leading cross-functional projects involving Legal, Regulatory Affairs, Sustainability, and other business functions
  • Experience representing an organization through trade associations and regulatory engagement
  • Bachelor’s degree in a relevant discipline

Responsibilities

  • Lead the identification and assessment of emerging sustainability and product-related policy developments
  • Serve as the subject matter expert on priority policy issues, providing analysis and advice to senior leaders
  • Establish and coordinate cross-functional teams to evaluate and respond to regulatory developments
  • Develop and support advocacy strategies on priority issues to protect Cytiva's interests

Key facts

Hard skills

Other skills

  • Advocacy
  • Communication
  • Analytical Thinking

About the company

Integrated DNA Technologies logo

Integrated DNA Technologies

Biotechnology

Integrated DNA Technologies, Inc. (IDT) develops, manufactures, and markets nucleic acid products for the life sciences industry in the areas of academic and commercial research, agriculture, medical diagnostics, and pharmaceutical development. IDT has developed proprietary technologies for genomic applications such as next generation sequencing, CRISPR genome editing, synthetic biology, digital PCR, and RNA interference. Through its GMP services, IDT manufactures products used by scientists researching many forms of cancer and most inherited and infectious diseases. IDT is widely recognized as an industry leader in custom nucleic acid manufacture, serving over 130,000 life sciences researchers. IDT was founded in 1987 in the United States and has its U.S. manufacturing headquarters in Coralville, Iowa, with additional U.S. manufacturing sites in San Diego, California; Research Triangle Park, North Carolina; and Ann Arbor, Michigan; with international sites in Leuven, Belgium and Singapore. *For research use only. Not for use in diagnostic procedures. Unless otherwise agreed to in writing, IDT does not intend these products to be used in clinical applications and does not warrant their fitness or suitability for any clinical diagnostic use. Purchaser is solely responsible for all decisions regarding the use of these products and any associated regulatory or legal obligations

Company details

Company typeLarge
IndustryBiotechnology
Company size1001-5000

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Job description


Bring more to life.


Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology?


At Cytiva, one of Danaher’s three platforms, our work helps to save lives—and we’re all united by a shared commitment to innovate for tangible impact. 


You’ll thrive in a culture of belonging where you and your unique viewpoint matter. And by harnessing Danaher’s system of continuous improvement, you help turn ideas into impact – innovating at the speed of life.


Working at Cytiva means being at the forefront of providing new solutions to transform human health. Our incredible customers undertake life-saving activities ranging from fundamental biological research to developing innovative vaccines, new medicines, and cell and gene therapies.


At Cytiva you will be able to continuously improve yourself and us – working on challenges that truly matter with people that care for each other, our customers, and their patients. Take your next step to an altogether life-changing career.


Learn about the Danaher Business System.


The Government Affairs Director, is responsible for identifying, assessing and helping shape emerging sustainability, chemicals and product-related policy developments that could materially impact Cytiva's business, products, operations and growth. The role facilitates cross-functional evaluation of regulatory risks and opportunities, coordinates company responses to significant policy changes, and supports the development of advocacy strategies that protect and advance Cytiva's long-term business interests.


This position reports to the Global Head of Government Affairs and Policy and is part of the Legal function and is expected to be located at one of our sites in Uppsala, Sweden, or Amersham, United Kingdom, with the possibility of a remote role based in Brussels.


What you will do:

  • Lead the identification and assessment of emerging sustainability, chemicals and product-related policy developments, translating complex regulatory changes into clear business implications and strategic recommendations.
  • Serve as the company's subject matter expert on priority policy issues, providing timely analysis and advice to senior leaders on risks, opportunities and potential business impacts.
  • Establish and coordinate cross-functional teams to evaluate and respond to significant regulatory developments, ensuring alignment across Government Affairs, Legal, Regulatory Affairs, Sustainability, Supply Chain and Commercial functions.
  • Develop and support advocacy strategies on priority issues, working closely with trade associations, industry coalitions and government affairs colleagues to help shape policy outcomes and protect Cytiva's interests.
  • Build and maintain effective relationships with key external stakeholders, including industry associations, regulators, policymakers and partner organisations, to strengthen the company's visibility and influence on critical policy issues.
  • Provide horizon scanning and early warning of emerging legislative, regulatory and geopolitical developments that could impact Cytiva's products, operations, supply chain or long-term growth strategy.

Who you are:

  • Long-standing experience in life sciences government affairs, public policy, regulatory affairs, sustainability policy, chemicals policy, environmental policy, or a related field, with a Bachelor’s degree in a relevant discipline.
  • Experience leading cross-functional projects or governance processes involving Legal, Regulatory Affairs, Sustainability, Supply Chain, Commercial or other business functions as well as experience of working with government affairs colleagues in different regions and juridictions in a multinational matrix organisation.
  • Experience representing an organization through life sciences trade associations, industry coalitions, government consultations, or regulatory engagement activities.
  • Experience working across multiple geographic regions, including Europe, North America and Asia-Pacific, on policy, regulatory or government affairs issues.
  • Experience supporting business responses to major regulatory or legislative changes, including cross-functional governance and implementation planning.

Cytiva, a Danaher Platform, offers a broad array of comprehensive, competitive benefit programs that add value to our lives. Whether it’s a health care program or paid time off, our programs contribute to life beyond the job. Check out our benefits at Danaher Benefits Info.

Join our winning team today. Together, we’ll accelerate the real-life impact of tomorrow’s science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life.

For more information, visit www.danaher.com.

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MR

Marcus Rivera

Chief Revenue Officer

m.rivera@company.com
linkedin.com/in/marcusrivera
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